ClinGen Allele Registry
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Canonical Allele Identifier:
CA1592773686
Gene: SAP30L-AS1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1582030351
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.154432028C>G , CM000667.2:g.154432028C>G
GRCh38
NC_000005.9:g.153811588C>G , CM000667.1:g.153811588C>G
GRCh37
NC_000005.8:g.153791781C>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_037897.1:n.204+11334G>C
Search 100 bp 5'
Search 100 bp 3'